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The influence of birth outcomes and pregnancy complications on interpregnancy interval: a quantile regression analysis.
Gebremedhin, Amanuel T; Regan, Annette K; Håberg, Siri E; Luke Marinovich, M; Tessema, Gizachew A; Pereira, Gavin.
Afiliação
  • Gebremedhin AT; Curtin School of Population Health, Curtin University, Perth, Western Australia, Australia. Electronic address: a.gebremedhin@curtin.edu.au.
  • Regan AK; Curtin School of Population Health, Curtin University, Perth, Western Australia, Australia; School of Population Health, Texas A&M University, College Station.
  • Håberg SE; Centre for Fertility and Health (CeFH), Norwegian Institute of Public Health, Oslo, Norway.
  • Luke Marinovich M; Curtin School of Population Health, Curtin University, Perth, Western Australia, Australia.
  • Tessema GA; Curtin School of Population Health, Curtin University, Perth, Western Australia, Australia.
  • Pereira G; Curtin School of Population Health, Curtin University, Perth, Western Australia, Australia; enAble Institute, Curtin University, Kent Street, Bentley, Western Australia, Australia; Centre for Fertility and Health (CeFH), Norwegian Institute of Public Health, Oslo, Norway.
Ann Epidemiol ; 85: 108-112.e4, 2023 09.
Article em En | MEDLINE | ID: mdl-37209928
PURPOSE: To ascertain whether adverse pregnancy outcomes at first pregnancy influence subsequent interpregnancy intervals (IPIs) and whether the size of this effect varies with IPI distribution METHODS: We included 251,892 mothers who gave birth to their first two singletons in Western Australia, from 1980 to 2015. Using quantile regression, we investigated whether gestational diabetes, hypertension, or preeclampsia in the first pregnancy influenced IPI to subsequent pregnancy and whether effects were consistent across the IPI distribution. We considered intervals at the 25th centile of the distribution as 'short' and the 75th centile as 'long'. RESULTS: The average IPI was 26.6 mo. It was 0.56 mo (95% CI: 0.25-0.88 mo) and 1.12 mo (95% CI: 0.56 - 1.68 mo) longer after preeclampsia, and gestational hypertension respectively. There was insufficient evidence to suggest that the association between previous pregnancy complications and IPI differed by the extent of the interval. However, associations with marital status, race/ethnicity and stillbirth contributed to either shortening or prolonging IPIs differently across the distribution of IPI. CONCLUSION: Mothers with preeclampsia and gestational hypertension had slightly longer subsequent IPIs than mothers whose pregnancies were not complicated by these conditions. However, the extent of the delay was small (<2 mo).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Complicações na Gravidez / Hipertensão Induzida pela Gravidez / Nascimento Prematuro Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Ann Epidemiol Assunto da revista: EPIDEMIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pré-Eclâmpsia / Complicações na Gravidez / Hipertensão Induzida pela Gravidez / Nascimento Prematuro Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Ann Epidemiol Assunto da revista: EPIDEMIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos